Infrared spectroscopy of 2-oxo-octanoic acid in multiple phases

Alpha-keto acids are environmentally and biologically relevant species whose chemistry has been shown to be influenced by their local environment. Vibrational spectroscopy provides useful ways to probe the potential inter- and intramolecular interactions available to them in several phases. We measu...

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Published inPhysical chemistry chemical physics : PCCP Vol. 24; no. 11; pp. 6757 - 6768
Main Authors Kappes, Keaten, Frandsen, Benjamin N, Vaida, Veronica
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 16.03.2022
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Summary:Alpha-keto acids are environmentally and biologically relevant species whose chemistry has been shown to be influenced by their local environment. Vibrational spectroscopy provides useful ways to probe the potential inter- and intramolecular interactions available to them in several phases. We measure and compare the IR spectra of 2-oxo-octanoic acid (2OOA) in the gas phase, solid phase, and at the air-water interface. With theoretical support, we assign many of the vibrational modes in each of the spectra. In the gas phase, two types of conformers are identified and distinguished, with the intramolecularly H-bonded form being the dominant type, while the second conformer type identified does not have an intramolecular hydrogen bond. The van der Waals interactions between molecules in solid 2OOA manifest C-H and C&z.dbd;O vibrations lower in energy than in the gas phase and we propose an intermolecular hydrogen bonding scheme for the solid phase. At the air-water interface the hydrocarbon tails of 2OOA do interact with each other while the carbonyls appear to interact with water in the subphase, but not with neighboring 2OOA as might be expected of a closely packed surfactant film. The chemistry defining inter- and intramolecular interactions available to 2-oxo-octanoic acid in environmentally relevant phases are spectroscopically probed.
Bibliography:10.1039/d1cp05345k
Electronic supplementary information (ESI) available. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1463-9076
1463-9084
DOI:10.1039/d1cp05345k